510(k) K121820 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
INWAVE
| Applicant | Zynex Medical, Inc., Lone Tree CO, US |
| Decision | Substantially Equivalent, Aug 24, 2012 |
| Received | Jun 21, 2012 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K121820
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.